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Journal Abstract Search

162 related items for PubMed ID: 7204104

  • 21. Hereditary spino-cerebellar degeneration and Ramsay-Hunt disease.
    Penneau D, Bigorgne JC, Fressinaud-Masdefeix L.
    Cah Med; 1974 Feb; 15(2):93-6. PubMed ID: 4848865
    [No Abstract] [Full Text] [Related]

  • 22. [Genesis of rapid eye movement disorder in spinocerebellar degeneration (author's transl)].
    Ozawa T, Ohba N, Tanino T.
    Nippon Ganka Gakkai Zasshi; 1977 Feb 10; 81(2):161-6. PubMed ID: 557884
    [No Abstract] [Full Text] [Related]

  • 23. [Clinical studies of spinocerebellar degeneration].
    Sohue I.
    Nihon Naika Gakkai Zasshi; 1984 Feb 10; 73(2):175-8. PubMed ID: 6427370
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  • 28. Celiac disease and spinocerebellar degeneration with normal vitamin E status.
    Ward ME, Murphy JT, Greenberg GR.
    Neurology; 1985 Aug 10; 35(8):1199-201. PubMed ID: 4022355
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  • 29. [Clinical observations on 2 cases of hereditary areflexic dystasia].
    Fabiani F.
    Riv Neurobiol; 1965 Aug 10; 11(2):219-27. PubMed ID: 5837065
    [No Abstract] [Full Text] [Related]

  • 30. Spino-cerebellar degeneration in Punjab.
    Jolly SS, Malhotra KC, Puri D.
    Neurol India; 1966 Aug 10; 14(3):120-4. PubMed ID: 5924718
    [No Abstract] [Full Text] [Related]

  • 31. "Lhermitte's sign" as a presenting symptom of subacute combined degeneration of the cord.
    Sandyk R, Brennan JW.
    Ann Neurol; 1983 Feb 10; 13(2):215-6. PubMed ID: 6830186
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  • 34. [Fluctuations of free fatty acids in the blood of patients with spinocerebellar degeneration].
    Ueda T.
    Rinsho Shinkeigaku; 1982 Oct 10; 22(10):909-17. PubMed ID: 7182093
    [No Abstract] [Full Text] [Related]

  • 35. [Scanning electron microscopy studies of erythrocytes in spinocerebellar degeneration].
    Yasuda Y, Akiguchi I, Shio H, Kameyama M.
    Rinsho Shinkeigaku; 1982 Jul 10; 22(7):644-50. PubMed ID: 7172533
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  • 36. [Spinocerebellar degeneration].
    Sobue I.
    Nihon Rinsho; 1978 May 10; Suppl():1714-5. PubMed ID: 691491
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  • 37. Neuromuscular changes in spinocerebellar degeneration.
    Itoga E, Kito S.
    Hiroshima J Med Sci; 1984 Sep 10; 33(3):311-21. PubMed ID: 6511456
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  • 39. [A family of familial amyloidosis with cerebellar ataxia and pyramidal tract sign--clinical and genetic study (author's transl)].
    Kobayashi T, Nakagawa S, Oguchi K, Yanagisawa N, Tsukagoshi H.
    Rinsho Shinkeigaku; 1978 Sep 10; 18(9):515-24. PubMed ID: 709971
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